Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Hillmen

Showing results (1-10 of 52) with videos related to

Pageof 6
Sort By:
Seminars in Hematology|June 13, 1998
Somatic mutation and clonal selection in the pathogenesis and in the control of paroxysmal nocturnal hemoglobinuriaM Bessler, P Hillmen
Molecular Pathology : MP|May 29, 2002
Paroxysmal nocturnal haemoglobinuria: nature's gene therapy?R J Johnson, P Hillmen
British Journal of Haematology|April 12, 2000
Implications of recent insights into the pathophysiology of paroxysmal nocturnal haemoglobinuriaP Hillmen, S J Richards
Blood|August 1, 1992
Clonal origin of abnormal granulocytes in paroxysmal nocturnal hemoglobinuriaM Bessler, P Hillmen, L Luzzatto
British Journal of Haematology|March 1, 1992
Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency in the red cells of patients with paroxysmal nocturnal haemoglobinuriaP Hillmen, J M Hows, L Luzzatto
Blood|November 9, 2000
Immunophenotypic analysis of B cells in PNH: insights into the generation of circulating naive and memory B cellsS J Richards, G J Morgan, P Hillmen
Lancet (London, England)|April 16, 1994
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuriaM Bessler, P Mason, P Hillmen, et al.
Cytometry|August 10, 2000
Application of flow cytometry to the diagnosis of paroxysmal nocturnal hemoglobinuriaS J Richards, A C Rawstron, P Hillmen
Somatic Cell and Molecular Genetics|March 1, 1993
Paroxysmal nocturnal hemoglobinuria: correction of abnormal phenotype by somatic cell hybridizationP Hillmen, M Bessler, J Bungey, et al.
Blood|October 9, 1999
Analysis of T cells in paroxysmal nocturnal hemoglobinuria provides direct evidence that thymic T-cell production declines with ageS J Richards, G J Morgan, P Hillmen
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
Seminars in Hematology|June 13, 1998
Somatic mutation and clonal selection in the pathogenesis and in the control of paroxysmal nocturnal hemoglobinuriaM Bessler, P Hillmen
Molecular Pathology : MP|May 29, 2002
Paroxysmal nocturnal haemoglobinuria: nature's gene therapy?R J Johnson, P Hillmen
British Journal of Haematology|April 12, 2000
Implications of recent insights into the pathophysiology of paroxysmal nocturnal haemoglobinuriaP Hillmen, S J Richards
Blood|August 1, 1992
Clonal origin of abnormal granulocytes in paroxysmal nocturnal hemoglobinuriaM Bessler, P Hillmen, L Luzzatto
British Journal of Haematology|March 1, 1992
Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency in the red cells of patients with paroxysmal nocturnal haemoglobinuriaP Hillmen, J M Hows, L Luzzatto
Blood|November 9, 2000
Immunophenotypic analysis of B cells in PNH: insights into the generation of circulating naive and memory B cellsS J Richards, G J Morgan, P Hillmen
Lancet (London, England)|April 16, 1994
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuriaM Bessler, P Mason, P Hillmen, et al.
Cytometry|August 10, 2000
Application of flow cytometry to the diagnosis of paroxysmal nocturnal hemoglobinuriaS J Richards, A C Rawstron, P Hillmen
Somatic Cell and Molecular Genetics|March 1, 1993
Paroxysmal nocturnal hemoglobinuria: correction of abnormal phenotype by somatic cell hybridizationP Hillmen, M Bessler, J Bungey, et al.
Blood|October 9, 1999
Analysis of T cells in paroxysmal nocturnal hemoglobinuria provides direct evidence that thymic T-cell production declines with ageS J Richards, G J Morgan, P Hillmen
Pageof 6